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Hydrochloric Acid → 4-Anilinophenyl hydrogen maleate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Maleic Anhydride | HCID 7923 | — |
| 反応物 | 4-Hydroxydiphenylamine | HCID 31208 | — |
| 反応物 | Potassium | HCID 5462222 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | tert-Butanol | HCID 6386 | — |
| 溶媒 | Potassium tert-butoxide | HCID 23665647 | — |
| 生成物 | 4-Anilinophenyl hydrogen maleate | HCID 70608900 | — |
反応手順
4-Anilinophenyl hydrogen maleate was prepared by adding 10 grams of maleic anhydride to a solution of the potassium salt of 4-anilinophenol which was prepared by dissolving 18.5 grams of 4-anilinophenol in a solution of potassium tert.butoxide prepared by reacting 3.9 grams of potassium with 75 milliliters of tert.butyl alcohol. The reaction mixture was stirred for 2 hours at 65°-70° C. and was then poured into a solution of 12 milliliters of concentrated hydrochloric acid in 138 milliliters of water. The organic layer was separated by extraction with benzene. The extract was washed twice with water and then allowed to evaporate. The residue was recrystallized twice from benzene yielding 1.3 grams of product which melted at 139°-142° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US03953411 |
| 出典データセット | uspto-grants-1976_04 |
| ORD ID | ord-3f33899e93004d5d81a08a275de29a58 |
| 出典メモ | uspto-grants-1976_04 |